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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1603190Erstellt: 26. Oktober 2026

Hydrochloric Acid → N-(p-azidobenzenesulfonyl) N'-(3-carboxypropionyl) cystamine

https://huagongshe.com/reaction/1603190

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktCystamine DihydrochlorideHCID 5941—
EduktSuccinic anhydrideHCID 7922—
EduktSodium HydroxideHCID 14798—
EduktN-(p-azidobenzenesulfonyl)-N'-(3-succinimidyloxycarbonyl-propionyl)cystamineHCID 19609028—
LösungsmittelWaterHCID 962—
ProduktN-(p-azidobenzenesulfonyl) N'-(3-carboxypropionyl) cystamineHCID 19609019—

Reaktionsschritte

2.2 g of cystamine dihydrochloride were dissolved in 20 ml of water and adjusted to pH 10 with NaOH. 2.1 g of p-azidobenzenesulfochloride were suspended in the solution and the mixture was stirred at room temperature for 5 hours. The precipitated N-(p-azidobenzenesulfonyl)cystamine was reacted with 2 g of succinic anhydride and stirred overnight. The resulting solution was acidified with HCl and the product was subsequently filtered off and washed with water. The residue was dried at room temperature in a high vacuum and gave 1.53 g of N-(p-azidobenzenesulfonyl)-N'-(3-carboxypropionyl)cystamine. The IR showed bands at 3283 (amide NH), 2134 (azide), 1714 (acid carbonyl), 1650 (amide), 1589+1547 (aromatic), 1284 (COOH), 1328+1180 (arylsulfonyl), 839 (p- disubst. benzene); TLC (silica gel: conc. NH3 (EtOH=1%). Rf=0.7; m.p. 163° (dec.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05986066
Quelldatensatzuspto-grants-1999_11
ORD IDord-1098af0e084b48738a80de62db0fe224
Quellennotizuspto-grants-1999_11